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  5. NDC Package Code: 72786-101-01 Oxbryta

NDC Package 72786-101-01 Oxbryta

Voxelotor Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
72786-101-01
Package Description:
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
72786-101
Proprietary Name:
Oxbryta
Non-Proprietary Name:
Voxelotor
Substance Name:
Voxelotor
Usage Information:
This medication is used to treat sickle cell disease. People with sickle cell disease have a certain abnormal protein (hemoglobin S) in their red blood cells that makes the cells stiff and irregularly shaped (sickle- or crescent moon-shaped). Voxelotor works by decreasing hemoglobin S. This effect may decrease symptoms such as tiredness, shortness of breath, and attacks of pain (sickle cell crisis).
11-Digit NDC Billing Format:
72786010101
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
90 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2265683 - voxelotor 500 MG Oral Tablet
  • RxCUI: 2265689 - OXBRYTA 500 MG Oral Tablet
  • RxCUI: 2265689 - voxelotor 500 MG Oral Tablet [Oxbryta]
  • RxCUI: 2265689 - Oxbryta 500 MG Oral Tablet
  • RxCUI: 2588070 - voxelotor 300 MG Tablet for Oral Suspension
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Global Blood Therapeutics, Inc, A Subsidiary Of Pfizer Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • VOXELOTOR 500 mg/1
    • Pharmacologic Class(es):
  • Cytochrome P450 3A4 Inhibitors - [MoA] (Mechanism of Action)
  • Hemoglobin S Polymerization Inhibitor - [EPC] (Established Pharmacologic Class)
  • Hemoglobin S Polymerization Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA213137
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-25-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 72786-101-01?

    The NDC Packaged Code 72786-101-01 is assigned to a package of 90 tablet, film coated in 1 bottle, plastic of Oxbryta, a human prescription drug labeled by Global Blood Therapeutics, Inc, A Subsidiary Of Pfizer Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 90 billable units per package.

    Is NDC 72786-101 included in the NDC Directory?

    Yes, Oxbryta with product code 72786-101 is active and included in the NDC Directory. The product was first marketed by Global Blood Therapeutics, Inc, A Subsidiary Of Pfizer Inc. on November 25, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 72786-101-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 90.

    What is the 11-digit format for NDC 72786-101-01?

    The 11-digit format is 72786010101. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-272786-101-015-4-272786-0101-01